Welcome to LookChem.com Sign In|Join Free
  • or
Benzene, 1,1'-(1,1,2,2-tetramethyl-1,2-ethanediyl)bis[4-(1-methylethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

33398-01-5

Post Buying Request

33398-01-5 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

33398-01-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33398-01-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,3,9 and 8 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 33398-01:
(7*3)+(6*3)+(5*3)+(4*9)+(3*8)+(2*0)+(1*1)=115
115 % 10 = 5
So 33398-01-5 is a valid CAS Registry Number.

33398-01-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[2,3-dimethyl-3-(4-propan-2-ylphenyl)butan-2-yl]-4-propan-2-ylbenzene

1.2 Other means of identification

Product number -
Other names 2,3-di-p-cumyl-2,3-dimethylbutane

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:33398-01-5 SDS

33398-01-5Downstream Products

33398-01-5Relevant academic research and scientific papers

Photochemistry of Some Deoxybenzoins in Micellar Solutions. Cage Effects, Isotope Effects, and Magnetic Field Effects

Turro, Nicholas J.,Mattay, Jochen

, p. 4200 - 4204 (2007/10/02)

The photolyses of 1,2-diphenyl-2-methyl-1-propanone (1) and its D-, 13C-, and alkyl-substituted derivatives 2-5 in various micellar solutions have been investigated.It was found that the extent of cage disproportionation to yield benzaldehydes 6 and α-methylstyrenes 7 is enhanced by a factor of about 10 compared to the photolyses in homogeneous organic solvents.The advantage of using micelles rather than homogeneous solutions to enhance the magnitude of magnetic isotope and magnetic field effects on cage disproportionation is demonstrated.The results are interpreted in terms of a mechanism involving the competition between hyperfine-induced intersystem crossing of a triplet radical pair (3RP) to form a singlet radical pair (1RP) and escape of 3RP from the micelle.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 33398-01-5